{"orpha":399685,"name":"Rare male infertility due to testicular endocrine disorder","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-399685/","orphanet_url":"https://www.orpha.net/en/disease/detail/399685","names":{"fr":{"name":"Infertilité masculine rare due à un trouble testiculaire endocrine"},"de":{"name":"Seltene Form der männlichen Infertilität durch endokrine testikuläre Störung"},"es":{"name":"Infertilidad masculina rara por un trastorno endocrino testicular"},"it":{"name":"Sterilità maschile rara da disfunzione endocrina testicolare"},"nl":{"name":"Zeldzame mannelijke onvruchtbaarheid door testiculaire endocriene stoornis"},"pt":{"name":"Infertilidade masculina rara devido a doença endócrina testicular"},"pl":{"name":"Rzadka niepłodność męska z powodu endokrynowych zaburzeń jąder"},"cs":{"name":"Vzácná mužská neplodnost způsobená testikulární endokrinní poruchou"},"uk":{"name":"Рідкісне чоловіче безпліддя, зумовлене ендокринним розладом яєчок"},"zh":{"name":"睾丸内分泌失调所致罕见男性不育"},"tr":{"name":"Testiküler endokrin bozukluğuna bağlı nadir erkek infertilitesi"}},"xrefs":[{"source":"MONDO","code":"18388","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681163","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":98312,"name":"OBSOLETE: Male infertility with impaired virilization due to a testicular disorder","status":"inactive"},{"type":"Referred to","orpha":98330,"name":"OBSOLETE: Male infertility with normal virilization due to androgen administration","status":"inactive"},{"type":"Referred to","orpha":98331,"name":"OBSOLETE: Male infertility with normal virilization due to a testicular defect","status":"inactive"}],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":399572,"name":"Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder","classifications":[201]},{"orpha":399983,"name":"Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin","classifications":[156]}],"children":[{"orpha":752,"name":"46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency","type":"Disease"},{"orpha":753,"name":"46,XY difference of sex development due to 5-alpha-reductase 2 deficiency","type":"Disease"},{"orpha":754,"name":"Androgen insensitivity syndrome","type":"Clinical group"},{"orpha":481,"name":"Kennedy disease","type":"Disease"},{"orpha":755,"name":"Leydig cell hypoplasia","type":"Disease"},{"orpha":181441,"name":"Rare disorder with hypergonadotropic hypogonadism","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}